Beneficial effect of capsaicin via TRPV4/EDH signals on mesenteric arterioles of normal and colitis mice

Graphical abstract

Highlights

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  Capsaicin induced vasorelaxation of human colonic submucosal arterioles in vitro and in vitro.

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  Capsaicin induced an endothelium-dependent vasorelaxation of human submucosal arterioles.

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  Capsaicin induced an endothelium-dependent vasorelaxation of mouse mesenteric arterioles.

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  Capsaicin induced vasorelaxation minily by TRPV1-mediated endothelial nitric oxide release.

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  Capsaicin induced vasorelaxation mainly by TRPV4/endothelium-dependent hyperpolarization.

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  Capsaicin exerted anti-colitis action in wide-type mice, but not in TRPV4 knock-out mice.

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  Capsaicin rescued the impaired endothelium-dependent vasorelaxation via TRPV4/EDH pathway.

Abstract

Introduction

Although capsaicin has long been used as food additive and medication worldwide, its actions on gastrointestinal tract as its most delivery pathway have not been well addressed.

Objectives

In the present study, we aimed to study GI actions of capsaicin on mesenteric arterioles in normal and colitis mice and to elucidate the underlying mechanisms.

Methods

Vasorelaxation of human submucosal arterioles and the mesenteric arterioles from wide-type (WT) mice, TRPV1 ^−/− and TRPV4 ^−/− (KO) mice were measured. The expression and function of TRPV channels in endothelial cells were examined by q-PCR, immunostaining, Ca ²⁺ imaging and membrane potential measurements.

Results

Capsaicin dose-dependently induced vasorelaxation of human submucosal arterioles and mouse mesenteric arterioles in vitro and in vivo through endothelium-dependent hyperpolarization (EDH), nitric oxide (NO), and prostacyclin (PGI ₂). Using TRPV1 and TRPV4 KO mice, we found that capsaicin-induced vasorelaxation was predominately through TRPV4/EDH, but marginally through TRPV1/NO/PGI ₂. Capsaicin induced hyperpolarization through activation of endothelial TRPV4 channels and intermediate-conductance of Ca ²⁺-activated K ⁺ channels to finally stimulate vasorelaxation. Importantly, capsaicin exerted anti-colitis action by rescuing the impaired ACh-induced vasorelaxation in WT colitis mice but not in TRPV4 KO colitis mice.

Conclusions

Capsaicin increases intestinal mucosal blood perfusion to potentially prevent/treat colitis through a novel TRPV4/EDH-dependent vasorelaxation of submucosal arterioles in health and colitis. This study further supports our previous notion that TRPV4/EDH in mesenteric circulation plays a critical role in the pathogenesis of colitis.